A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349079



Internal ID21006632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:8017204..8021366hg38UCSC Ensembl
chr2:8157334..8161496hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg384163
hg194163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18091061
Samples
Known GenesLINC00299
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349079
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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